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"Idiopathic Eosinophilic Vasculitis": Another Side of Hypereosinophilic Syndrome? A Comprehensive Analysis of 117 Cases in Asthma-Free Patients.

Authors :
Lefèvre G
Leurs A
Gibier JB
Copin MC
Staumont-Sallé D
Dezoteux F
Chenivesse C
Lopez B
Terriou L
Hachulla E
Launay D
Etienne N
Labalette M
DeGroote P
Pontana F
Quemeneur T
Hatron PY
Schleinitz N
Viallard JF
Hamidou M
Martin T
Morati-Hafsaoui C
Groh M
Lambert M
Kahn JE
Source :
The journal of allergy and clinical immunology. In practice [J Allergy Clin Immunol Pract] 2020 Apr; Vol. 8 (4), pp. 1329-1340.e3. Date of Electronic Publication: 2019 Dec 18.
Publication Year :
2020

Abstract

Background: The absence of asthma may rule out a diagnosis of eosinophilic granulomatosis with polyangiitis in patients with hypereosinophilic syndrome (HES) and features of vasculitis.<br />Objective: To describe eosinophilic vasculitis (EoV) as a possible manifestation of HES in asthma-free patients.<br />Methods: We screened our hospital database and the literature for patients with HES who met the following 4 criteria: (1) histopathological or clinical features of EoV (biopsy-proven vasculitis with predominant eosinophilic infiltration of the vessel wall and/or features of vasculitis with tissue and/or blood hypereosinophilia [absolute eosinophil count >1.5 G/L]); (2) no other obvious causes of reactive eosinophilia, organ damage, and vasculitis; (3) the absence of antineutrophil cytoplasmic antibodies; and (4) the absence of current asthma.<br />Results: Ten of our 83 (12%) asthma-free patients with HES and 107 additional cases in the literature met the criteria for EoV. After a critical analysis of the patients' clinical and laboratory characteristics and outcomes, we identified 41 cases of single-organ EoV (coronary arteritis, n = 29; temporal arteritis, n = 8; cerebral vasculitis, n = 4). Of the remaining 76 patients with EoV, the most frequent manifestations (>10%) were cutaneous vasculitis (56%), peripheral neuropathy (24%), thromboangiitis obliterans-like disease (16%), fever (13%), central nervous system involvement (13%), deep venous thrombosis (12%), and nonasthma lung manifestations (12%). Blood hypereosinophilia more than 1.5 G/L was observed in 79% of patients, and necrotizing vasculitis was observed in 44%.<br />Conclusions: Our results suggest that idiopathic EoV (HES-associated vasculitis) can be classified as an eosinophilic-rich, necrotizing, systemic form of vasculitis that affects vessels of various sizes in asthma-free patients.<br /> (Copyright © 2019 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
2213-2201
Volume :
8
Issue :
4
Database :
MEDLINE
Journal :
The journal of allergy and clinical immunology. In practice
Publication Type :
Academic Journal
Accession number :
31863912
Full Text :
https://doi.org/10.1016/j.jaip.2019.12.011